Prader–Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review

Prader–Willi syndrome (PWS) is a complex genetic disorder with three PWS molecular genetic classes and presents as severe hypotonia, failure to thrive, hypogonadism/hypogenitalism and developmental delay during infancy. Hyperphagia, obesity, learning and behavioral problems, short stature with growt...

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Detalles Bibliográficos
Autor principal: Butler, Merlin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002205/
https://www.ncbi.nlm.nih.gov/pubmed/36901699
http://dx.doi.org/10.3390/ijms24054271

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002205/
https://www.ncbi.nlm.nih.gov/pubmed/36901699
http://dx.doi.org/10.3390/ijms24054271

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